Variant (rsID / SNP)
rs1130609
rs1130609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RRM2. Location: chromosome 2, position 10,262,920. The table records no clinical significance for this variant.
Reference-table entries
RRM2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:10262920
- HGVS
- NM_001165931.1,c.175T>G,p.Ser59Ala
- Allele change
- Missense_S59A
Associated conditions / phenotypes
Leukemia|Leukemia, Acute Myeloid|Myeloid Leukemia|Endocervical Adenocarcinoma|Cervical Cancer|Cervical Squamous Cell Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.